Instramed DUALMAX, Руководство пользователя

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User Manual | Safety information
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WARNING: the patient must be completely still during the cardiac rhythm
analysis phase (aed mode). do not give cardiac massage at this point.
ATTENTION: do not use DualMax or its accessories in the presence of MRI
equipment.
This equipment was projected to offer resistance to electromagnetic
interferences. However, the functioning of this device can be affected in the
present of strong sources of electromagnetic-interference or radio-frequency,
such as mobile phones, communicator radios, etc.
If the precision of measurements seems to be incorrect, first check the vital
signs of the patient and then check the functioning of the DualMax.
WARNING: always check the general state of the equipment, the battery and
the accessories before using it.
Before installing the equipment verify if there are any abnormalities or
damage caused by mishandling during transportation.
NOTICE: the DualMax must only be used as a complement to assess the
patient’s physiological conditions. It must be accompanied by constant
analysis of the patient’s clinical status and symptoms.
WARNING: The use of the DualMax is restricted to one patient at a time.
NOTICE: the applied parts (electrodes, sensors, armbands, etc.) are protected
against defibrillation discharge; during discharge there may be baseline
variation.
WARNING: when the DualMax is operated in monitor mode, it can be used
with other electromedical equipment simultaneously connected to the
patient, provided that the other equipment are in compliance with the safety
standards.
WARNING: the conductive parts of the electrodes and connectors associated
with the applied parts, including the neutral electrode, must not come into
contact with other conductive parts, including the ground wire.
NOTICE: avoid connecting the patient to several items of equipment at the
same time. The limits of current leakage may be exceeded.
NOTICE: the applied parts intended to come into contact with the patient have
been evaluated and comply with the directives and principles of ISO 10993-1.
NOTICE: when removing the equipment from its package, carefully verify if
there is any abnormality or visible damage in the device or its accessories,
caused by impact or mishandling during transportation. In case of
irregularities, please contact Instramed.
NOTICE: disposable accessories and any other components must be
disposed of according to the norms of hospital waste disposal.
WARNING: Do not modify this equipment without authorization from
Instramed.